GROUPE SOBER SAS
FR-MF-000017818 · France · SAINT GEORGES DE RENEINS
GROUPE SOBER SAS is registered in the European database on medical devices as a manufacturer, with 1 155 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 155 |
|---|
Most frequent device types declared: ACC. TALONNETTE TOESHOES EVOLUTIVE, ATTELLE DE POIGNET/MAIN COMPLEX, CEINTURE DE MAINTIEN ABDO AU FAUTEUIL, CEINTURE LOMBAIRE H21, CHAUSSURE POST-OPERATOIRE DE L’AVANT-PIED.
Devices declared under this manufacturer
- CRYOSTAB® OMNI-WALKER PACK
- FYN WRIST
- GOT - TS
- SIMULATEUR VIEILLISSEMENT BRAS
- STABICOUD 3D
- STABICOUD MODULO 90° - TS
- STABIL AJOUREE - H21 - T4
- STABILIG 3 CLIQ
- STABILIG CENTRO
- STABILITY ABDO - TU
- STABIPOIGNET 3D LONG
- STABIPOIGNET COMPLEX CARE - TXL/G
Showing 12 of 1 155 declared devices.
Catalogue references include FYN WRIST, GOT, SIMULATEUR VIEILLISSEMENT BRAS, STABIL AJOUREE H21, STABILIG CENTRO, STABILITY ABDO.
European nomenclature codes declared: M030501, Y063303, Y061209, Y060403, Y060612, Y060406.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 155 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 1 155 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. GROUPE SOBER SAS was not found in either the U.S. or the Canadian register.